...
首页> 外文期刊>Applied and Environmental Microbiology >Noncovalent Immobilization of Streptavidin on In Vitro- and In Vivo-Biotinylated Bacterial Magnetic Particles
【24h】

Noncovalent Immobilization of Streptavidin on In Vitro- and In Vivo-Biotinylated Bacterial Magnetic Particles

机译:链霉亲和素在体内和体内生物素化细菌磁性颗粒上的非共价固定

获取原文
           

摘要

Biotinylated magnetic nanoparticles were constructed by displaying biotin acceptor peptide (BAP) or biotin carboxyl carrier protein (BCCP) on the surface of bacterial magnetic particles (BacMPs) synthesized by Magnetospirillum magneticum AMB-1. BAP-displaying BacMPs (BAP-BacMPs) were extracted from bacterial cells and incubated with biotin and Escherichia coli biotin ligase. Then the in vitro biotinylation of BAP-BacMPs was confirmed using alkaline phosphatase-labeled antibiotin antibody. In contrast, BacMPs displaying the intact 149 residues of AMB-1 BCCP (BCCP-BacMPs) and displaying the COOH-terminal 78 residues of BCCP (BCCP78-BacMPs) were biotinylated in AMB-1 cells. The in vivo biotinylation of BCCP-BacMPs and BCCP78-BacMPs was thought to be performed by endogenous AMB-1 biotin ligase. Streptavidin was introduced onto biotinylated BacMPs by simple mixing. In an analysis using tetramethyl rhodamine isocyanate-labeled streptavidin, approximately 15 streptavidin molecules were shown to be immobilized on a single BCCP-BacMP. Furthermore, gold nanoparticle-BacMP composites were constructed via the biotin-streptavidin interaction. The conjugation system developed in this work provides a simple, low-cost method for producing biotin- or streptavidin-labeled magnetic nanoparticles. Various functional materials can be site selectively immobilized on these specially designed BacMPs. By combining the site-selective biotinylation technology and the protein display technology, more innovative and attractive magnetic nanomaterials can be constructed.
机译:通过在由Magnetospirillum magneticum AMB-1合成的细菌磁性颗粒(BacMP)的表面上展示生物素受体肽(BAP)或生物素羧基载体蛋白(BCCP),构造生物素化的磁性纳米颗粒。从细菌细胞中提取展示BAP的BacMP(BAP-BacMP),并与生物素和大肠杆菌生物素连接酶孵育。然后使用碱性磷酸酶标记的抗生物素抗体确认BAP-BacMPs的体外生物素化。相反,展示完整的149个AMB-1 BCCP残基的BacMPs(BCCP-BacMPs)和展示BCCP的COOH末端78个残基的BacMP(BCCP78-BacMPs)在AMB-1细胞中被生物素化。 BCCP-BacMPs和BCCP78-BacMPs的体内生物素化被认为是由内源性AMB-1生物素连接酶完成的。通过简单的混合将链霉亲和素引入生物素化的BacMP上。在使用四甲基若丹明异氰酸酯标记的抗生蛋白链菌素的分析中,大约15个抗生蛋白链菌素分子被固定在单个BCCP-BacMP上。此外,金纳米粒子-BacMP复合材料是通过生物素-链霉亲和素相互作用构建的。在这项工作中开发的偶联系统为生产生物素或链霉亲和素标记的磁性纳米粒子提供了一种简单,低成本的方法。可以将各种功能材料选择性地固定在这些特殊设计的BacMP上。通过结合位点选择性生物素化技术和蛋白质展示技术,可以构建更具创新性和吸引力的磁性纳米材料。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号